Evidence map›Paper›PMID 42573633›Full record

ReviewVirchows Archiv : an international journal of pathology2026

Management of high-risk (B3) breast lesions in symptomatic practice: evidence review and practical recommendations for multidisciplinary care.

Emad A Rakha, Abeer Shaaban, Giuseppe Floris, Grace Callagy, Nisha Sharma, Raghavan Vidya, Thomas Decker, Peter Regitnig, Yazan Masannat, Elena Provenzano and 22 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Virchows Archiv : an international journal of pathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

32 authors.

Emad A RakhaSchool of Medicine, University of Nottingham, Nottingham, UK. emadrakha@yahoo.com.
Abeer ShaabanCellular Pathology, Queen Elizabeth Hospital Birmingham, Birmingham, UK.
Giuseppe FlorisDepartment of Pathology, University Hospitals Leuven, KU-Leuven, Herbstreit 49, Leuven, 3000, Belgium.
Grace CallagyDiscipline of Pathology, University of Galway, Galway, Ireland.
Nisha SharmaBreast Radiologist, Breast Unit, University of Galway, Galway, Ireland.
Raghavan VidyaOncoplastic Breast Surgery Department, The Royal Wolverhampton NHS Trust, Wolverhampton, UK.
Thomas DeckerReference Centers Mammography, Münster and Berlin, Berlin, Germany.
Peter RegitnigDiagnostic and Research Institute of Pathology, Medical University of Graz, Graz, Austria.
Yazan MasannatOncoplastic Breast Surgery Department, Broomfield Hospital, Mid and South Essex NHS Trust, Chelmsford, England.
Elena ProvenzanoDepartment of Histopathology, Addenbrookes Hospital, Cambridge, UK.
Rahul DebDepartment of Pathology, University Hospitals of Derby and Burton, Derby, UK.
Jill R DietzDepartment of Surgery, NYULangone Health Medical Center, New York, NY, USA.
Basel AltrabulsiPathology and Laboratory Medicine Institute, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates.
William TehRadiology Department, Northwick Park Hospital & Royal Free Breast Screening, Harrow, Middlesex, UK.
Muna A AbuhejlehDepartment of Pathology, National Reference Laboratory and Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates.
Zsuzsanna VargaDepartment of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.
Paul van DiestDepartment of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
Gábor CserniDepartment of Pathology, Albert Szent-Györgyi Faculty of Medicine, University of Szeged, Bács-Kiskun County Teaching Hospital, Szeged, Kecskemét, Hungary.
Maria Pia FoschiniDepartment of Biomedical and Neuromotor Sciences, Unit of Pathology at Bellaria Hospital, University of Bologna, Bologna, 40139, Italy.
Carolien H M van DeurzenDepartment of Pathology, Erasmus MC, Rotterdam, The Netherlands.
Madhuri WarrenDepartment of Cellular Pathology, Barts Health NHS Trust, Queen Mary University of London, London, UK.
Yasmeen MirDepartment of Pathology, Liverpool University Hospitals Group, Liverpool, UK.
Emmanuelle Charafe-JauffretPathology Department & Epithelial Stem Cells and Cancer Lab, CRCM, Inserm, CNRS, Institut Paoli-Calmettes, Aix-Marseille Univ, Equipe labellisée LIGUE contre le cancer, Marseille, France.
Soha El SheikhResearch Department of Pathology, University College London, London, UK.
Zsuzsanna Bago-HorvathDepartment of Pathology, Medical University of Vienna, Vienna, Austria.
Isabella CastellanoDepartment of Medical Sciences, University of Turin, Turin, Italy.
Stephen GrobmyerSurgical Department Breast Oncoplastic Unit, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates.
Mieke R Van BockstalDepartment of Pathology, UCLouvain, Cliniques universitaires Saint-Luc, Brussels, Belgium.
Puay Hoon TanLuma Medical Centre, Royal Square Medical Centre, Singapore, Singapore.
Cecily QuinnDepartment of Histopathology, School of Medicine, Irish National Breast Screening Programme, St. Vincent's University Hospital, University College Dublin, Dublin, Ireland.
Sarah PinderSchool of Cancer and Pharmaceutical Sciences, King's College London, London, UK.
UK National Coordinating Committee for Breast Pathology and the European Working Group for Breast Screening Pathology

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Borderline breast lesions (B3 lesions, also termed lesions of uncertain malignant potential or high-risk lesions) represent a heterogeneous group of entities associated with variable risks of malignancy. While the management of screen-detected B3 lesions has become increasingly standardised, no dedicated international recommendations exist for symptomatic B3 lesions, despite them posing a distinct clinical challenge. Symptomatic lesions differ from screen-detected lesions in their mode of presentation, lesion characteristics, biopsy techniques, and diagnostic objectives; consequently, management strategies derived from screening populations may not be directly applicable. This review summarises the current evidence and proposes a pragmatic management framework for B3 lesions encountered in the symptomatic setting (defined as those presenting with breast symptoms outside population-based screening programmes). This is particularly relevant for patients under 50 years of age, where the primary objective is to exclude malignancy at the index site rather than solely to stratify long-term cancer risk. Clinical-radiological-pathological concordance and multidisciplinary assessment are central to management decisions. Lesions presenting as palpable abnormalities (which are typically larger) or those demonstrating radiological-pathological discordance warrant a lower threshold for additional sampling or excision. Conversely, selected concordant lesions without atypia may be managed conservatively following adequate sampling. The long-term cancer risk associated with epithelial atypia should also be considered with subsequent risk-based surveillance implemented where appropriate. Overall, management requires a risk-adapted, multidisciplinary approach integrating pathological, radiological, and clinical factors alongside patient symptoms and quality-of-life considerations. Given the limited evidence, current recommendations rely on expert consensus and a proposed practical framework. They underscore the need for large-scale, high-quality studies with long-term follow-up to establish formal clinical guidelines.

Indexed as

B3 breast lesionsMultidisciplinary approachRadiological-pathological correlationSymptomatic breast lesion managementVacuum-assisted biopsyVacuum-assisted excision

Identifiers

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.